TCF7L2, transcription factor 7 like 2, 6934

N. diseases: 257; N. variants: 70
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 0.953 190 2006 2020
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 0.908 65 2006 2020
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 1.000 37 2006 2020
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.100 1.000 35 2006 2020
dbSNP: rs7901695
rs7901695
0.851 0.160 10 112994329 intron variant T/C snv 0.34
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.900 1.000 23 2006 2020
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.100 0.944 18 2007 2019
dbSNP: rs290487
rs290487
0.776 0.280 10 113149972 intron variant C/T snv 0.16
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 0.667 15 2007 2015
dbSNP: rs11196205
rs11196205
0.827 0.200 10 113047288 intron variant G/A;C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.800 0.917 12 2006 2020
dbSNP: rs11196218
rs11196218
0.925 0.160 10 113080735 intron variant G/A snv 0.25
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 0.700 10 2007 2015
dbSNP: rs4506565
rs4506565
0.790 0.280 10 112996282 intron variant A/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.870 0.900 10 2006 2020
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.100 0.900 10 2008 2019
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.090 1.000 9 2006 2016
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.090 1.000 9 2006 2016
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.090 0.444 9 2007 2017
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 9 2012 2019
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.870 0.875 8 2008 2018
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.070 0.857 7 2007 2019
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
Nutritional and Metabolic Diseases 0.070 1.000 7 2006 2020
dbSNP: rs11196172
rs11196172
0.708 0.200 10 112967084 intron variant G/A snv 0.13
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.820 0.833 6 2014 2019
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.060 1.000 6 2012 2018
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.060 1.000 6 2012 2018
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.060 0.833 6 2008 2017
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.050 1.000 5 2008 2018
dbSNP: rs12255372
rs12255372
0.667 0.480 10 113049143 intron variant G/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.050 1.000 5 2008 2018
dbSNP: rs7903146
rs7903146
0.554 0.680 10 112998590 intron variant C/G;T snv
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.800 1.000 5 2009 2019